{{Rsnum
|rsid=191807913
|Gene=NPHS1
|Chromosome=19
|position=35844371
|Orientation=plus
|GMAF=0.0009183
|Gene_s=NPHS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ClinVar
|ALT=C,T
|CAF=0.9991; 0.0009183; .
|CHROM=19
|CLNACC=RCV000049871.1
|CLNALLE=2
|CLNDBN=Finnish congenital nephrotic syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0403399:256300:839:197601003
|CLNHGVS=NC_000019.9:g.36335273G>T
|CLNSIG=4
|COMMON=1
|Disease=Finnish congenital nephrotic syndrome
|FwdALT=C,T
|FwdREF=G
|GENEINFO=NPHS1:4868
|GENE_ID=4868
|GENE_NAME=NPHS1
|REF=G
|RSPOS=36335273
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050268000000000016110100
|WGT=0
|dbSNPBuildID=135
|rsid=191807913
}}{{PMID Auto
|PMID=20172850
|Title=Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS).
|OA=1
}}